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3059-23-2

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3059-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3059-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3059-23:
(6*3)+(5*0)+(4*5)+(3*9)+(2*2)+(1*3)=72
72 % 10 = 2
So 3059-23-2 is a valid CAS Registry Number.

3059-23-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl meso-α,α'-diphenylsuccinate

1.2 Other means of identification

Product number -
Other names diethyl d,l-α,α'-diphenylsuccinate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3059-23-2 SDS

3059-23-2Relevant articles and documents

Kofron,Hauser

, p. 2085 (1970)

-

Tokuda,M. et al.

, p. 621 - 624 (1975)

-

Thioether- and sulfone-functionalized dibenzopentalenes as n-channel semiconductors for organic field-effect transistors

Hermann, Mathias,Wu, Ruihan,Grenz, David C.,Kratzert, Daniel,Li, Hanying,Esser, Birgit

, p. 5420 - 5426 (2018)

Dibenzo[a,e]pentalenes (DBPs) are promising candidates to be used as ambipolar or n-type semiconductors in organic field-effect transistors (OFETs). For n-channel conduction, low LUMO energy levels are required. Furthermore, a close molecular packing in t

Convenient synthetic methods to C2 symmetric 3,4-diphenylpyrrolidines

Rao, Vutukuri Dharma,Periasamy, Mariappan

, p. 703 - 706 (2007/10/03)

Convenient methods of synthesis of racemic and optically pure 3,4- diphenylpyrrolidine derivatives, involving oxidative coupling of ethyl phenylacetate using TiCl4/Et3N and reduction of the dl-2,3-diphenylsuccinic acid or the corresponding cyclic imide with NaBH4/I2 reagent in crucial steps, are described.

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